Methyl 3-amino-5-bromo-4-iodobenzoate
97%
- Product Code: 44930
CAS:
1341291-68-6
| Molecular Weight: | 355.96 g./mol | Molecular Formula: | C₈H₇BrINO₂ |
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| EC Number: | MDL Number: | MFCD17276540 | |
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| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile intermediate for the preparation of more complex compounds. Its structure, featuring both bromo and iodo substituents, makes it particularly valuable in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in pharmaceutical and material science research. The ester group allows for further functionalization, enabling the synthesis of amides or other derivatives. Additionally, its amino group provides a reactive site for modifications, making it useful in the development of dyes, agrochemicals, and bioactive molecules. Its halogenated aromatic ring also lends itself to applications in the production of liquid crystals and organic electronic materials.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 G | 10-20 days | ฿2,952.00 |
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| 0.250 G | 10-20 days | ฿5,904.00 |
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Methyl 3-amino-5-bromo-4-iodobenzoate
This chemical is primarily utilized in organic synthesis as a versatile intermediate for the preparation of more complex compounds. Its structure, featuring both bromo and iodo substituents, makes it particularly valuable in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in pharmaceutical and material science research. The ester group allows for further functionalization, enabling the synthesis of amides or other derivatives. Additionally, its amino group provides a reactive site for modifications, making it useful in the development of dyes, agrochemicals, and bioactive molecules. Its halogenated aromatic ring also lends itself to applications in the production of liquid crystals and organic electronic materials.
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